BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    TERUMO DIGITAL CLINICAL THERMOMETER

    K Number: K841740 · Decision Jul 18, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    488
    Registration Numbers
    488
    Same Product Code
    797
    Applicant Total
    143
    Review Days
    82

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    Basic Information

    Device Name
    TERUMO DIGITAL CLINICAL THERMOMETER
    K Number
    K841740
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.2910
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Terumo Medical Corp.
    Date Received
    April 27, 1984
    Decision Date
    July 18, 1984
    Product Code
    FLL
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FLL Continuous Measurement Thermometer

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    Other Clearances by Terumo Medical Corp.

    K Number Device Name
    K111606 PINNACLE PRECISION ACCESS SYSTEM
    K111556 GLIDECROSS SUPPORT CATHETER
    K110540 TERUMO SUPPORT CATHETER
    K102008 GLIDESHEATH
    K091329 PINNACLE DESTINATION PERIPHERAL GUIDING SHEATH
    K082997 TERUMO HYBRIA CLOSED SYSTEM SAFETY I.V. CATHETER
    K090040 RADIFOCUS GLIDECATH (OR RADIFOCUS GLIDECATH XP)
    K082847 PINNACLE ROII INTRODUCER SHEATH
    K082519 FINECROSS MG CORONARY MICRO-GUIDE CATHETER
    K082736 RADIFOCUS OPTITORQUE ANGIOGRAPHIC CATHETER
    Search all 143 clearances from Terumo Medical Corp. →